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FDA 510(k) Applications Submitted by MARK G URBANSKI
FDA 510(k) Number
Submission Date
Device Name
Applicant
K990019
01/04/1999
DRG MEDIUM SCREW SYSTEM
DOLPHIN MEDICAL TECHNOLOGIES, INC.
K960533
02/07/1996
K3 BONE SCREW SYSTEM
KINETIKOS MEDICAL, INC.
K960537
02/07/1996
K2 BONE SCREW SYSTEM
KINETIKOS MEDICAL, INC.
K960539
02/07/1996
DIAO HAND SURGERY SET
KINETIKOS MEDICAL, INC.
K960692
02/20/1996
SUBTALAR MBA SYSTEM
KINETIKOS MEDICAL, INC.
K961051
03/11/1996
UNIVERSAL TOTAL WRIST SYSTEM (MODIFICATION)
KINETIKOS MEDICAL, INC.
K973810
10/07/1997
DRG LARGE SCREW SYSTEM
DOLPHIN MEDICAL TECHNOLOGIES, INC.
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